Canonical Allele Identifier: CA1201917066
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1570942139

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484221C>G , CM000663.2:g.159484221C>G GRCh38
NC_000001.10:g.159454011C>G , CM000663.1:g.159454011C>G GRCh37
NC_000001.9:g.157720635C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1237C>G
XR_922189.3:n.690+1237C>G